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SEQanswers: an open access community for collaboratively decoding genomes

Summary: The affordability of high-throughput sequencing has created an unprecedented surge in the use of genomic data in basic, translational and clinical research. The rapid evolution of sequencing technology, coupled with its broad adoption across biology and medicine, necessitates fast, collabor...

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Detalles Bibliográficos
Autores principales: Li, Jing-Woei, Schmieder, Robert, Ward, R. Matthew, Delenick, Joann, Olivares, Eric C., Mittelman, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3338018/
https://www.ncbi.nlm.nih.gov/pubmed/22419780
http://dx.doi.org/10.1093/bioinformatics/bts128
Descripción
Sumario:Summary: The affordability of high-throughput sequencing has created an unprecedented surge in the use of genomic data in basic, translational and clinical research. The rapid evolution of sequencing technology, coupled with its broad adoption across biology and medicine, necessitates fast, collaborative interdisciplinary discussion. SEQanswers provides a real-time knowledge-sharing resource to address this need, covering experimental and computational aspects of sequencing and sequence analysis. Developers of popular analysis tools are among the >4000 active members, and ~40 peer-reviewed publications have referenced SEQanswers. Availability: The SEQanswers community is freely accessible at http://SEQanswers.com/ Contact: david.mittelman@vt.edu; ecolivares@gmail.com Supplementary information: Supplementary data are available at Bioinformatics online.